Status:

COMPLETED

Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subjects With Dry Eye Disease

Lead Sponsor:

Allergan

Conditions:

Dry Eye Syndromes

Eligibility:

All Genders

18+ years

Phase:

PHASE3

Brief Summary

This study will evaluate the safety, efficacy, and acceptability of an eye drop formulation in subjects with dry eye disease.

Eligibility Criteria

Inclusion

  • Dry eyes
  • Current use of eye drops for dry eye at least twice daily, on average for at least 3 months

Exclusion

  • Cataract, laser-assisted in situ keratomileusis (LASIK), or photorefractive keratectomy (PRK) surgery in the last 12 months
  • Need to wear contact lenses during the study, or has worn contact lenses in the last 6 months
  • Active ocular allergy

Key Trial Info

Start Date :

October 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 15 2012

Estimated Enrollment :

315 Patients enrolled

Trial Details

Trial ID

NCT01459588

Start Date

October 1 2011

End Date

February 15 2012

Last Update

April 16 2019

Active Locations (1)

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Petaluma, California, United States

Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subjects With Dry Eye Disease | DecenTrialz